58652-54-3

Basic information

• Product Name: 1-adamantyl trifluoroacetate
• Synonyms: 1-adamantyl trifluoroacetate
• CAS NO: 58652-54-3
• Molecular Weight: 248.245
• Mol File: 58652-54-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-adamantyl trifluoroacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-adamantyl trifluoroacetate(58652-54-3)
• EPA Substance Registry System: 1-adamantyl trifluoroacetate(58652-54-3)

Safety Data

• Hazardous Substances Data: 58652-54-3(Hazardous Substances Data)

Upstream product

• 768-90-1 1-Adamantyl bromide 
• 2712-78-9 bis-[(trifluoroacetoxy)iodo]benzene 
• 768-93-4 1-iodoadamantane 
• 281-23-2 adamantane 
• 76-05-1 trifluoroacetic acid 
• 27184-84-5 chromyl trifluoroacetate 

Downstream Products

• 880-52-4 N-(1-adamantyl)acetamide 
• 768-95-6 1-adamanthanol 
• 208262-17-3 (3s,5s,7s)-N-(3-nitrophenyl)adamantan-1-amine 
• 160917-92-0 N-(1-adamantyl)-2-nitroaniline 
• 59974-48-0 1-(4-amino-3-nitrophenyl)adamantane 
• 56714-80-8 (3s,5s,7s)-N-(4-nitrophenyl)adamantan-1-amine 
• 78872-15-8 C₁₆H₂₀OSe 
• 281-23-2 adamantane 
• 23906-87-8 1-dichlorophosphinoyladamantane 
• 1459-55-8 4-(1-adamantyl)toluene 
• 88459-01-2 (1s,3s)-adamantan-1-yl(phenyl)sulfide 
• 75480-69-2 1-(phenylseleno)tricyclo<3.3.1.1^3,7>decane 
• 51812-97-6 p-ethyl-(1-adamantyl)benzene 
• 135394-82-0 1-<(pentafluorophenyl)thio>tricyclo<3.3.1.1^3,7>decane 

Relevant articles and documents

Efficient oxidation of adamantanes by sodium nitrite with molecular oxygen in trifluoroacetic acid

Oxidation of adamantanes by oxygen was effectively achieved by use of sodium nitrite as a catalyst in trifluoroacetic acid (TFA) to give 1-adamantyl trifluoroacetates, from which adamantanols were obtained in good yields. A catalytic amount of sodium nitrite was essential and TFA was the best solvent among solvents examined for this oxidation. Georg Thieme Verlag Stuttgart.

Oxidative Displacement of Halogen from Alkyl Halides by Phenyliodine(III) Dicarboxylates

The reaction of alkyl iodides with aryliodine(III) dicarboxylates affords as the main product the ester derived through substitution of iodine by an acyloxy group; in some cases α-iodoalkyl esters are also formed along with other minor products.Certain reactive bromides and chlorides react along similar lines.The mechanism of these reactions is briefly discussed.